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首页> 外文期刊>Trials >Single dose of intravenous ferric carboxymaltose infusion versus multiple fractionated doses of intravenous iron sucrose in the treatment of postoperative anaemia in colorectal cancer patients: study protocol for a randomised controlled trial
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Single dose of intravenous ferric carboxymaltose infusion versus multiple fractionated doses of intravenous iron sucrose in the treatment of postoperative anaemia in colorectal cancer patients: study protocol for a randomised controlled trial

机译:单剂量的静脉内碳滤菌糖输注与多种分馏剂量的静脉内铁蔗糖治疗结肠直肠癌患者术后贫血:用于随机对照试验的研究方案

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Patients with colorectal cancer (CRC) often present with associated anaemia which is usually present at the time of diagnosis and is aggravated during the postoperative period due to blood loss during the surgery process. Several guidelines advocate for the treatment of postoperative anaemia in these patients in order to prevent complications and allogeneic blood transfusions. However, there are no publications to shed light on the effectiveness of intravenous iron (IVI) administration after CRC surgery and the optimal dose and regimen. We have started a clinical trial with the objective of comparing the effectiveness of 1000?mg of ferric carboxymaltose with fractionated iron sucrose 200?g/48?h for the treatment of postoperative anaemia, by measuring the change of haemoglobin (Hb) levels from postoperative day (POD) 1 to POD 30. We designed an open label randomised controlled trial to compare two postoperative IVI treatment regimens. Patients aged ?18?years undergoing CRC surgery, with Hb??11?g/dL on POD 1 are randomly assigned to receive either 1000?mg of ferric carboxymaltose (single dose) or 200?g/48?h of iron sucrose. The main study endpoint will be the change from POD 1 to POD 30 in Hb levels and the key secondary endpoint the percentage of patients with Hb levels ≥?13?g/dL at POD 30. Other secondary endpoints include: changes in iron metabolism parameters (Fe, ferritin, transferrin, % saturated trasferrin) at POD 30; total doses of iron received; number of postoperative transfusions; compliance with oral iron treatment; number of medical and surgical complications; adverse reactions reported by the patient; use of health resources after surgery; and changes in quality of life (QoL). It has been estimated that a sample of 48 patients per group will allow detecting a difference of 0.75?g/dL in Hb in the change in Hb levels from POD 1 to POD 30. The results of this study will confirm if the single dose of 1000?mg ferric carboxymaltose should be preferred in front of the fractionated doses and in which type of patients this regimen should be used preferably. European Union Clinical Trials Register, EudraCT 2015-001005-13 . Registered on 6 January 2015.
机译:患有结肠直肠癌(CRC)的患者通常存在于诊断时通常存在的相关性贫血,并且在手术过程中由于失血而在术后期间加剧。若干指导方针倡导这些患者术后贫血的治疗,以防止并发症和同种异体输血。然而,在CRC手术和最佳剂量和方案之后,没有出版物对静脉注射铁(IVI)给药的有效性。我们已经开始了临床试验,其目的是将1000毫克碳滤器的有效性与分级的铁蔗糖200?G /48αh进行比较,通过测量术后血红蛋白(HB)水平的血红蛋白(HB)水平的术后血症天(POD)1到POD 30.我们设计了一个开放标签随机对照试验,以比较两个术后IVI治疗方案。患者患者> 18?年龄在CRC手术中,随机分配了Hbα<α1Ω·11μg/ dl,以接收1000×mg铁羧酰符(单剂量)或200?G / 48?蔗糖。主要研究终点将是从Pod 1到Pod 30的变化在Hb水平中,关键次级端点Hb水平≥13Ω·克/ DL的百分比≥13​​Ω·克/ dL。其他次级端点包括:铁代谢参数的变化(Fe,铁蛋白,转铁蛋白,饱和曲脂蛋白)在豆荚30处;收到的总剂量的铁;术后输血的数量;遵守口服熨斗治疗;医疗和手术并发症的数量;患者报告的不良反应;手术后使用健康资源;和生活质量的变化(QOL)。据估计,每组48名患者的样品将使HB的Hb中的0.75μg/ dL的差异从Pod 1到Pod 30中的差异检测到0.75Ωg/ dl。该研究的结果将确认单剂量是否为单剂量1000?Mg Ferric Carboxymaltose应该在分级剂的前面优选,并且在哪种患者中,应优选使用该方案。欧盟临床试验登记册,eudract 2015-001005-13。 2015年1月6日注册。

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